bumetanide 1 mg
INDICATIONS AND USAGE Bumetanide tablets are indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including the nephrotic syndrome. Almost equal diuretic response occurs after oral and parenteral administration of bumetanide. Therefore, if impaired gastrointestinal absorption is suspected or oral administration is not practical, bumetanide should be given by the intramuscular or intravenous route. Successful treatment with bumetanide tablets following instances of allergic reactions to furosemide suggests a lack of cross-sensitivity.
heritage pharmaceuticals inc. d/b/a avet phar
ROUND WHITE 701
701 ROUND WHITE
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HOW SUPPLIED
BUMEtanIDE Tablets USP are available as white to off-white, round, flat-faced, beveled edge, unscored tablet debossed with “701” on one side and plain on the other, containing 1 mg
BUMEtanIDE, USP packaged in bottles of 100 tablets (NDC 23155-901-01), 500 tablets (NDC 23155-901-05) and 1000 tablets (NDC 23155-901-10).
BUMEtanIDE Tablets USP are available as white to off-white, round, flat-faced, beveled edge, unscored tablet debossed with “702” on one side and plain on the other, containing 2 mg
BUMEtanIDE, USP packaged in bottles of 100 tablets (NDC 23155-902-01), 500 tablets (NDC 23155-902-05) and 1000 tablets (NDC 23155-902-10). Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Distributed by: Avet Pharmaceuticals Inc. East Brunswick, NJ 08816 1.866.901.DRUG (3784) 51U000000468US01 Revised: 05/2024 logo
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